PTSD Clinical Trials
76 studies are recruiting for ptsd in the United States right now. Each one is listed on ClinicalTrials.gov, the public registry the research teams themselves file with. TrialBoost is not a doctor, a research site, or a study sponsor: the research team decides who takes part.
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Studies, page 3
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State-Funded Trial Assessing Recovery and Long-Term Impact of Guided Psilocybin for Healing Trauma
The principal investigator for this study plans to build upon the psilocybin-assisted therapy intervention used in prior completed trials to conduct an open-label trial of two psilocybin administration sessions combined with psychotherapy to investigate the safety, tolerability, and clinical effica…
- Stage
- Phase 2
- Ages
- 21 to 64
- Site
- Baylor College of Medicine, Houston, Texas
- Run by
- Baylor College of Medicine
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Neural Connectivity During Therapy for Adolescent PTSD
Posttraumatic stress disorder in adolescence impairs neurobiological networks underlying cognitive, social and emotional skills. Neuroimaging research that seeks to identify the neural mechanisms of treatments for PTSD could lead to novel treatments, but progress has been slow using current methods…
- Stage
- Not phased
- Ages
- 12 to 17
- Site
- UT Health Department of Psychiatry, San Antonio, Texas
- Run by
- The University of Texas Health Science Center at San Antonio
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Art Therapy and Emotional Well Being in Military Populations With Posttraumatic Stress Symptoms
Art therapy is used across the Military Health System for treatment of posttraumatic symptoms, but there is limited research on how art therapy is able to restore emotional expression and regulation in service members. This research hopes to learn about the effects of art therapy on emotional expre…
- Stage
- Not phased
- Ages
- 18 to 64
- Site
- National Intrepid Center of Excellence, Bethesda, Maryland
- Locations
- 2 in total
- Run by
- Walter Reed National Military Medical Center
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Adaptive Decision-making And Personalized Treatment for PTSD (ADAPT-PTSD)
By doing this research project, the investigators hope to learn which strategies work best to help veterans who are not benefiting from their first PTSD treatment or not completing between-session homework assignments regularly that might improve treatment response. The investigators also want to l…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- Augusta VA, Augusta, Georgia
- Locations
- 4 in total
- Run by
- The University of Texas Health Science Center at San Antonio
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Recovery Through Inhibitory Learning, Self-Efficacy Building, Problem Solving, and Community Building
This is a two-part study to develop and test a brief, virtual therapy program for lesbian, gay, bisexual, transgender, and queer (LGBTQ+) people who have experienced trauma and use alcohol. Phase 1: You'll be invited to share your perspective to help make the program relevant, inclusive, and affirm…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- University of Rhode Island, Providence, Rhode Island
- Run by
- University of Rhode Island
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Determining the Benefits of Exercise on Cardiovascular Risk in PTSD
The purpose of this study is to use a non-invasive imaging technique called positron emission tomography/magnetic resonance imaging (PET/MRI) to investigate the effects of exercise on brain activity and arterial (blood vessel) inflammation in people with PTSD symptoms and evidence of or elevated ri…
- Stage
- Not phased
- Ages
- 18 to 65
- Site
- Massachusetts General Hospital, Boston, Massachusetts
- Run by
- Massachusetts General Hospital
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Patient Outcome Reporting for Timely Assessments of Life With Post-Traumatic Stress Disorder
This study aims to implement and evaluate a more timely approach to post-traumatic stress disorder (PTSD) diagnosis and management, entitled Patient Outcome Reporting for Timely Assessments of Life with Post-Traumatic Stress Disorder (PORTAL-PTSD) in a primary care setting with a high prevalence of…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- CFHC South Chicago, Chicago, Illinois
- Locations
- 2 in total
- Run by
- University of Chicago
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Post-Traumatic Stress Disorder Focused Psychodynamic Psychotherapy
This is a randomized controlled trial of Trauma-Focused Psychodynamic Psychotherapy (TFPP) in comparison with TAU (at the VA) in a 2:1 ratio in 75 Veterans with PTSD who have not responded to standard treatment at the VA.
- Stage
- Not phased
- Ages
- 18 to 70
- Site
- VA New York Harbor Healthcare System - Manhattan Campus, New York, New York
- Run by
- Montefiore Medical Center
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PTSD Screening in Pregnant Black Women
This study will compare the effectiveness of two active screening interventions in improving post-traumatic stress disorder (PTSD) symptoms, maternal perinatal care utilization, satisfaction utilization of mental healthcare services, and maternal health and birth-related outcomes for Black pregnant…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- Grady Health System, Atlanta, Georgia
- Locations
- 2 in total
- Run by
- Emory University
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Comparing Telehealth to In-person a Combined Metacognitive Training in Veterans With mTBI/PTSD
Veterans with mild traumatic brain injury (mTBI) and post-traumatic stress disorder (PTSD) commonly experience cognitive impairments including attention and executive function deficits that interfere with their ability to engage in productive personal and social activities. Of the limited intervent…
- Stage
- Not phased
- Ages
- 30 to 55
- Site
- North Florida/South Georgia Veterans Health System, Gainesville, FL, Gainesville, Florida
- Run by
- VA Office of Research and Development
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Preventing the Development of Chronic Pain: Treating PTSD at Acute Pain Onset
Although most people recover from acute pain (such as pain caused by injury, surgery, repetitive motion, or unknown causes), many people do not fully recover and will experience chronic pain. Untreated posttraumatic stress disorder (PTSD) appears to be a key risk factor for the transition from acut…
- Stage
- Not phased
- Ages
- 18 to 70
- Site
- Rush University Medical Center, Chicago, Illinois
- Run by
- Rush University Medical Center
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Hybrid Type 1 Randomized Pilot Trial of a Peer-led Family and Social Strengthening Group Intervention for Refugee Families
The proposed study draws on prior research to evaluate the feasibility, acceptability and explore preliminary effectiveness of Coffee and Family Education and Support, Version (CAFES2) using a pilot randomized type 1 hybrid effectiveness-implementation design. CAFES2 is a peer-led family and social…
- Stage
- Not phased
- Ages
- 12 to 55
- Site
- University of Illinios Chicago, Chicago, Illinois
- Run by
- University of Illinois at Chicago
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Self-Management Interventions After an ICD Shock
This study, "Biobehavioral Intervention to Reduce PTSD Symptoms After an ICD Shock," addresses a critical need in cardiology care by describing the feasibility and acceptability of a timely, highly promising, electronically-delivered intervention for patients who have recently received an ICD deliv…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- University of Washington, Seattle, Washington
- Run by
- University of Washington
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Determining the Right Acupuncture for Good Recovery Over Neuropsychiatric Trauma
This study seeks to verify that a specific acupuncture treatment is effective at reducing symptoms of neuropsychiatric trauma found in those diagnosed with Post-Traumatic Stress Disorder (PTSD).
- Stage
- Not phased
- Ages
- 18 to 74
- Site
- Mike O'Callaghan Military Medical Center, Nellis Air Force Base, Nevada
- Run by
- Paul Crawford
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MDMA-assisted Cognitive Processing Therapy Versus Cognitive Processing Therapy for Veterans With Severe Posttraumatic Stress Disorder
In partnership with the Veterans Affairs (VA) Palo Alto Health Care System and Stanford University, this study aims to evaluate clinical outcomes, assess implementation feasibility, and health economics of MDMA-assisted Cognitive Processing Therapy (MDMA-aCPT) in the treatment of posttraumatic stre…
- Stage
- Phase 2
- Ages
- 18 and older
- Site
- VA Palo Alto Health Care System / Stanford University, Palo Alto, California
- Run by
- Patricia Suppes
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Project Safe Guard-Trauma
The goal of this randomized controlled trial is to determine if a counseling intervention, Project Safe Guard-Trauma (PSG-T), increases secure firearm storage practices in adults who screen positive for posttraumatic stress disorder (PTSD). The main questions this study aims to answer are: * Does P…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- University of Colorado Anschutz Medical Campus, Aurora, Colorado
- Run by
- University of Colorado, Denver
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Glecaprevir/Pibrentasvir for Post-traumatic Stress Disorder
A double-blind randomized placebo-controlled trial to further investigate glecaprevir/pibrentasvir (GLE/PIB), a direct acting antiviral (DAA) that has been associated with posttraumatic stress disorder (PTSD) symptom improvement when prescribed for the treatment of chronic hepatitis C viral infecti…
- Stage
- Phase 2
- Ages
- 19 to 70
- Site
- White River Junction VAMC, White River Junction, Vermont
- Run by
- White River Junction Veterans Affairs Medical Center
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A Comparative Effectiveness Study of PTSD Treatments Among Sexual and Gender Minority Populations
The goal of this clinical trial is see if Cognitive Processing Therapy and STAIR Narrative Therapy work to treat posttraumatic stress disorder (PTSD) among lesbian, gay, bisexual, transgender, queer/questioning, intersex, asexual/aromantic, and all other sexual or gender minority (LGBTQIA+) adults.…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- Stanford University, Palo Alto, California
- Locations
- 2 in total
- Run by
- Stanford University
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NYSCF Scientific Discovery Biobank
The New York Stem Cell Foundation (NYSCF) Research Institute is performing this research to accelerate diverse disease research using cells from the body (such as skin or blood cells) to make stem cells and other types of cells, conduct research on the samples, perform genetic testing, and store th…
- Stage
- Not phased
- Ages
- 0 and older
- Site
- New York Stem Cell Foundation Research Institute, New York, New York
- Run by
- New York Stem Cell Foundation Research Institute
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The Effect of Outpatient Ketamine Infusion on Chronic Neuropathic Pain and PTSD
This study is aimed to evaluate outpatient ketamine infusion within a military chronic neuropathic pain population and its effect on PTSD. Currently, this is a pilot study with 30 participants. Participants will be randomized to (1) a moderate dose ketamine, (2) moderate dose ketamine +Mg, or (3) a…
- Stage
- Phase 4
- Ages
- 18 to 70
- Site
- Brooke Army Medical Center, San Antonio, Texas
- Run by
- Margaux M. Salas, PhD
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Evaluation of the H.O.O.V.E.S. Healing Intensives Program
The aim of this study is to measure the impact of these H.O.O.V.E.S. healing intensives on Veteran participants using several psychological instruments. The investigators are planning to administer the demographic questionnaires and psychological instruments to Veteran participants before the heali…
- Stage
- Not phased
- Ages
- 18 to 120
- Site
- George E. Wahlen Department of Veterans Affairs Medical Center, Salt Lake City, Utah
- Run by
- VA Salt Lake City Health Care System
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Biomarkers in the Retina for Prognosticating Mental Health Treatments
Title: ERG as a potential biomarker of SSRI-responsive PTSD: A pilot study Posttraumatic stress disorder (PTSD) affects many individuals who experience a traumatic event. Previous studies suggest that there is a connection between the brain and the retina, and that the electroretinogram (ERG) may b…
- Stage
- Not phased
- Ages
- 21 to 75
- Site
- VA Puget Sound Health Care System, Seattle, Washington
- Run by
- VA Puget Sound Health Care System
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Targeting the Default Mode Network: A TMS-fMRI Study
In post-traumatic stress disorder (PTSD), intrusive, traumatic, autobiographical memories lead to anxiety symptoms. Recent work suggests a new repetitive pulse transcranial magnetic stimulation (rTMS) brain target that might bring relief. Since this proposed target is not well understood, the goal …
- Stage
- Not phased
- Ages
- 18 to 55
- Site
- VA Palo Alto, Palo Alto, California
- Run by
- Allyson Rosen
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The Influence of Aerobic Exercise on Consolidation of Fear Extinction Learning in PTSD
This study aims to test whether aerobic exercise performed after fear extinction learning improves cognitive, physiological, and neural indices of extinction recall in a sample of trauma-exposed men and women with and without posttraumatic stress disorder (PTSD). Participants will complete a clinic…
- Stage
- Not phased
- Ages
- 18 to 64
- Site
- Wade Hall - University of Alabama, Tuscaloosa, Alabama
- Run by
- University of Alabama, Tuscaloosa
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Improving Therapeutic Learning for PTSD
The proposed project seeks to demonstrate the engagement of post-exposure dopamine neurotransmission and downstream acute reorganization of dopaminergic resting-state neural networks as a means of increasing consolidation of extinction memories formed during analogue exposure therapy in adult women…
- Stage
- Phase 2
- Ages
- 21 to 50
- Site
- University of Texas, Austin, Texas
- Locations
- 2 in total
- Run by
- University of Wisconsin, Madison
How to read this page. Every study here comes from ClinicalTrials.gov, the public registry that research teams are required to file with. We have summarised each one in plain language and shown where it is running. We have not changed what any study says it is doing.
What TrialBoost is. We help people find research that might suit them, and, if they ask us to, we pass their details to the research team running it. We are not a doctor, a research site, or a study sponsor, and we do not decide who takes part in anything. Joining costs nothing and you can change your mind at any point.
Paid placement. Some studies pay us when someone asks to be connected to them. Those are labelled Sponsored wherever they appear, and they only appear when they match what you were actually looking for.